Caterpillar CTP056030U

GUDID 00801741175565

Caterpillar Arterial Embolization Device, 0.056 Inch ID Catheter Compatibility

CLEARSTREAM TECHNOLOGIES LIMITED

Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic Non-neurovascular embolization plug, metallic

• Primary Device ID: 00801741175565
• NIH Device Record Key: fc917955-45aa-4474-b48e-84f9f11fa902
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Caterpillar
• Version Model Number: CTP056030U
• Catalog Number: CTP056030U
• Company DUNS: 989214291
• Company Name: CLEARSTREAM TECHNOLOGIES LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741175565 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191532

FDA Product Code

• KRD: Device, Vascular, for Promoting Embolization

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-02-18
• Device Publish Date: 2020-02-10

On-Brand Devices [Caterpillar]

• 00801741175565: Caterpillar Arterial Embolization Device, 0.056 Inch ID Catheter Compatibility
• 00801741155307: Caterpillar Micro Arterial Embolization Device, 0.027 Inch ID Catheter Compatibility
• 00801741155314: Caterpillar Arterial Embolization Device, 0.038 Inch ID Catheter Compatibility